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QVANTIMETRIC 2KAPPA AND LAMBDA TEST KIT

K852999 Class II Traditional
Decision Date
1985-10-21
Sponsor / Applicant
Kallestad Laboratories, Inc.

Technical Specification

510(k) Submission ID K852999
Product Code DEH
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5550
Decision Date 1985-10-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

QVANTIMETRIC 2KAPPA AND LAMBDA TEST KIT received FDA 510(k) clearance under submission number K852999, sponsored by Kallestad Laboratories, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 1985-10-21.

Classification & Regulation

This clearance is catalogued under FDA product code DEH and 21 CFR 866.5550, within the Immunology review panel as a Class II device.